2,3-Diaminopropionic acid

L-2,3-Diaminopropanoic acid
Names
IUPAC name
(2S)-2,3-Diaminopropanoic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
Properties
C3H8N2O2
Molar mass 104.11 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

2,3-Diaminopropionic acid (2,3-diaminopropionate) is a non-proteinogenic amino acid found in certain secondary metabolites, including zwittermicin A[1] and tuberactinomycin.[2]

Biosynthesis

2,3-Diaminopropionate is formed by the pyridoxal phosphate (PLP) mediated amination of serine.

Biosynthesis of L-2,3 Diaminopropionate

References

  1. ↑ Rogers EW, Molinski TF (February 2007). "Asymmetric synthesis of diastereomeric diaminoheptanetetraols. A proposal for the configuration of (+)-zwittermicin a". Org. Lett. 9 (3): 437–40. PMC 2729442 Freely accessible. PMID 17249781. doi:10.1021/ol062804a.
  2. ↑ Michael G. Thomas (2003). "ADeciphering Tuberactinomycin Biosynthesis: Isolation, Sequencing, and Annotation of the Viomycin Biosynthetic Gene Cluster". Antimicrob Agents Chemother. 47 (9): 2823–2830. PMC 182626 Freely accessible. PMID 12936980. doi:10.1128/AAC.47.9.2823-2830.2003.
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